Canonical Allele Identifier: CA519538982
Gene:

Linked Data

MyVariant Identifiers: chrY:g.7548822A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680781A>T , CM000686.2:g.7680781A>T GRCh38
NC_000024.9:g.7548822A>T , CM000686.1:g.7548822A>T GRCh37
NC_000024.8:g.7608822A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.533A>T